4.4 Article

Phenotypic and genotypic changes in obesity and type 2 diabetes of male KK mice with aging

Journal

EXPERIMENTAL ANIMALS
Volume 71, Issue 1, Pages 71-81

Publisher

INT PRESS EDITING CENTRE INC
DOI: 10.1538/expanim.21-0109

Keywords

age-related changes; glucose metabolism; KK strain; lipid metabolism; model mouse

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Research on preventing and treating age-related metabolic diseases is crucial due to the aging population. The use of elderly diabetic mouse models, such as the male KK mice, can be beneficial in studying the deterioration of glucose and lipid metabolism. However, the utility of KK mice as models for studying aging related to obesity and diabetes is unclear. This study investigates age-related changes in glucose and lipid metabolism in male KK mice fed a standard diet and suggests the need to induce deterioration in these mice through breeding with high-sucrose or high-fat diets in order to create a more useful elderly obese and diabetic animal model.
Research into the prevention and treatment of age-related metabolic diseases are important in the present-day situation of the aging population. We propose that an elderly diabetic mouse model may be useful to such research as it exhibits deterioration of glucose and lipid metabolism. Although the KK mouse strain is commonly used as a model of moderate obesity and type 2 diabetes, the utility of this strain as an elderly obese and diabetic model mouse for research into aging remains unclear. The present study aimed to investigate age-related changes of glucose and lipid metabolism in male KK mice fed a standard chow diet. We demonstrate that 40 weeks KK mice exhibit age-related dysfunctions, such as development of insulin resistance associated with pancreatic islet hypertrophy and decreased lipolysis in white adipose tissue (WAT) compared with 15 weeks KK mice. However, aging does not appear to cause mitochondrial dysfunction of brown adipose tissue. Unexpectedly, hyperglycemia, potential glucose uptake in insulin-sensitive organs, hepatic lipid accumulation, hypertrophy of adipocytes, and inflammation in epididymal WAT did not worsen but rather compensated in 40 weeks KK mice. Our data indicate that the use of male KK mice as an elderly obese and diabetic mouse model has some limitations and in order to represent a useful elderly obese and diabetic animal model, it may be necessary to induce deterioration of glucose and lipid metabolism in KK mice through breeding with high-sucrose or high-fat diets.

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